Benign copy number changes in clinical cytogenetic diagnostics by array CGH
Benign copy number changes in clinical cytogenetic diagnostics by array CGH is a scholarly work, published in 2008 in ''Cytogenetics and Genome Research''. The main subjects of the publication include genome, concordance, genetics, polyploidy, comparative genomic hybridization, bioinformatics, Copy number analysis, breakpoint, genomics, biology, copy-number variation, computational biology, and population. A database of apparently benign copy number variants (bCNVs) detected by a Spectral Genomics Inc./PerkinElmer BAC array platform has been maintained through the University of Utah Comparative Genomic Hybridization laboratory since 2005.